Departments of Cardiology The First Affiliated Hospital of Nanjing Medical University Nanjing Jiangsu China.
Department of Biostatistics School of Public Health Nanjing Medical University Nanjing Jiangsu China.
J Am Heart Assoc. 2022 Aug 16;11(16):e025058. doi: 10.1161/JAHA.121.025058. Epub 2022 Aug 5.
Background Insulin receptor substrate-1 () rs956115 is associated with vascular risk in patients with coronary artery disease and concomitant diabetes. (rs4244285) modulates clopidogrel response and predicts the outcome of coronary artery disease. This study was designed to explore the association between , genotypes, platelet reactivity, and 1-year outcome in patients with coronary artery disease undergoing percutaneous coronary intervention. Methods and Results Genotyping was performed using an improved multiplex ligation detection reaction technique. Platelet aggregation was assessed by light transmission aggregometry. Major adverse cardiovascular events were defined as a composite of cardiovascular death, myocardial infarction, and ischemic stroke. A total of 2213 consecutive patients were screened and 1614 were recruited. At 1 month, patients with CG genotype had significantly lower levels of ADP-induced platelet aggregation compared with patients with CC homozygotes. Patients with CG or GG genotype had a 2.09-fold higher risk of major adverse cardiovascular events compared with those with CC homozygotes (95% CI, 1.04-4.19; =0.0376). By comparison, patients with GA or AA genotype had higher ADP-induced platelet aggregation compared with patients with GG homozygotes. Although there was no significant difference in risk of major adverse cardiovascular events between patients with GA/AA and GG genotypes, patients with GA genotype had a 2.19-fold higher risk than those with GG homozygotes (95% CI, 1.13-4.24; =0.0200). No interaction between and genotypes was observed. Conclusions In patients following percutaneous coronary intervention, GG/CG and GA genotypes were associated with 2.09- and 2.19-fold increased cardiovascular risk, respectively, at 1-year follow-up. The association between genotypes and major adverse cardiovascular events appeared to be independent of known clinical predictors. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT01968499.
胰岛素受体底物-1(IRS-1)rs956115 与伴有糖尿病的冠心病患者的血管风险相关。(rs4244285)调节氯吡格雷的反应,并预测冠心病的结果。本研究旨在探讨 IRS-1 基因多态性与经皮冠状动脉介入治疗的冠心病患者血小板反应性及 1 年预后的关系。
采用改良多重连接检测反应技术进行基因分型。采用透光比浊法检测血小板聚集。主要不良心血管事件定义为心血管死亡、心肌梗死和缺血性卒中的复合事件。共筛选 2213 例连续患者,纳入 1614 例。在 1 个月时,CG 基因型患者 ADP 诱导的血小板聚集水平明显低于 CC 纯合子患者。与 CC 纯合子患者相比,CG 或 GG 基因型患者发生主要不良心血管事件的风险增加 2.09 倍(95%CI,1.04-4.19;=0.0376)。相比之下,GA 或 AA 基因型患者的 ADP 诱导血小板聚集水平高于 GG 纯合子患者。尽管 GA/AA 和 GG 基因型患者发生主要不良心血管事件的风险无显著差异,但 GA 基因型患者的风险较 GG 纯合子患者增加 2.19 倍(95%CI,1.13-4.24;=0.0200)。未观察到 IRS-1 基因型与 基因型之间存在交互作用。
在经皮冠状动脉介入治疗后的患者中,1 年后 GG/CG 和 GA 基因型分别与心血管风险增加 2.09 倍和 2.19 倍相关。IRS-1 基因型与主要不良心血管事件之间的关系似乎独立于已知的临床预测因素。